chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	3973584	3973585	C	T	15	INTERGENIC	homozygous	45729931
20	3973621	3973622	C	T	19	INTERGENIC	homozygous	45729932
20	3974483	3974484	G	T	4	INTERGENIC	homozygous	45729934
20	3974490	3974491	T	TAATCTTATTCTTATCCCTCTCCCCCTCCCCTGCACCTCCTCCTCCTCCTCCTCCTCCTCCTCCCTTTTTAGTATAGACTTTATTC	2	INTERGENIC	homozygous	45838300
20	3975748	3975749	C	T	17	INTERGENIC	possibly homozygous	45729936
20	3977387	3977388	G	A	9	INTERGENIC	possibly homozygous	45729940
20	3977388	3977389	G	A	9	INTERGENIC	possibly homozygous	45729941
20	3977637	3977638	G	A	12	INTERGENIC	possibly homozygous	45729942
20	3974720	3974721	A	AAGT	9	INTERGENIC	possibly homozygous	45818325
20	3978055	3978056	A	G	14	GENIC	possibly homozygous	45374393
20	3978119	3978120	A	G	3	GENIC	heterozygous	45729943
20	3978136	3978137	C	A	2	GENIC	homozygous	45729944
20	3978137	3978138	C	T	2	GENIC	homozygous	45729945
20	3978173	3978174	A	G	9	GENIC	possibly homozygous	45729946
20	3978265	3978266	C	A	22	GENIC	heterozygous	45729947
20	3978442	3978443	T	C	5	GENIC	homozygous	45729948
20	3978842	3978843	T	C	15	INTERGENIC	homozygous	45729949